Uroplakin III is not a major candidate gene for primary vesicoureteral reflux

被引:26
作者
Kelly, H
Ennis, S
Yoneda, A
Bermingham, C
Shields, DC
Molony, C
Green, AJ
Puri, P
Barton, DE [1 ]
机构
[1] Our Ladys Hosp Sick Children, Natl Ctr Med Genet, Dublin 12, Ireland
[2] Our Ladys Hosp Sick Children, Childrens Res Ctr, Dublin 12, Ireland
[3] Natl Univ Ireland Univ Coll Dublin, Dept Med Genet, Dublin 4, Ireland
[4] Natl Univ Ireland Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
[5] Royal Coll Surgeons Ireland, Dept Clin Pharmacol, Dublin 2, Ireland
[6] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
关键词
vesicoureteral reflux; uroplakin; genetic linkage;
D O I
10.1038/sj.ejhg.5201322
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vesicoureteral reflux (VUR) is the retrograde flow of urine from the bladder into the ureter and towards the kidneys. VUR is the most common cause of end stage renal failure in both children and adults and it is a major cause of severe hypertension in children. VUR is seen in approximately 1 - 2% of newborn Caucasians. Substantial evidence exists that VUR is a genetic disorder. Uroplakins are integral membrane proteins found in the bladder wall. Knockout studies in mice have suggested uroplakin III (UPK3) as a candidate gene for VUR. We have used parametric and nonparametric linkage analysis and tests for association, to investigate this possibility in a cohort of 126 sibling pairs affected with primary VUR. None of the analyses showed any substantial evidence for linkage or association of markers at the UPK3 locus to VUR. Our results do not support a role for UPK3 in primary VUR.
引用
收藏
页码:500 / 502
页数:3
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